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Serotonin Abnormalities in Dravet Syndrome Mice Before and After the Age of Seizure Onset

Dravet syndrome (DS) is a genetic form of severe epilepsy often associated with mutation of the SCN1A gene encoding the voltage gated sodium channel Nav1.1. Typically refractive to conventional therapy, serotonin neurotransmission may be an innovative target for treatment. To further understand the...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Brain Res
Prif Awduron: Hatini, Paul G., Commons, Kathryn G.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2019
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC6922539/
https://ncbi.nlm.nih.gov/pubmed/31445030
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2019.146399
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